Southland Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Southland Instruments, Inc. makes
Southland Instruments, Inc. manufactures bone marrow needles for aspiration procedures and biopsy/aspiration trays designed to support the collection of bone marrow samples.
These devices are classified as Class I under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Lee Bone Marrow Needles Ref K842106
Regimes: 510(k) Registry: 510(k)Lee Bone Marrow Biopsy/Aspiration Tray Ref K852897
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Southland Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Southland Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Southland Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Southland Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Southland Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Southland Instruments, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Southland Instruments, Inc. in the registry?
The most recently registered devices listed for Southland Instruments, Inc. include LEE BONE MARROW NEEDLES and LEE BONE MARROW BIOPSY/ASPIRATION TRAY.